Table 1. Macromolecule-production information.
| Source organism | L. rhamnosus GG (ATCC 53103) |
| DNA source | L. rhamnosus GG (ATCC 53103) |
| Forward primer† | 5′-CCACATTGGGTTCAGAATTCTGATCAAACTG |
| Reverse primer‡ | 5′-TGCGCCAATCGGACTCGAGCGGCAAATAAC |
| Cloning vector | pET-28b(+) (Novagen) |
| Expression vector | pET-28b(+) (Novagen) |
| Expression host | E. coli BL21 (DE3) pLysS |
| Complete amino-acid sequence of the construct produced§ | MGRDPNSDQTAEIVIHKRIYRDIRQPEDVWYENDGHRIDPNNPDKDGYKLLSKTSGLNGANFEVYDASSLLKPNMTPEAIRALVDRYQNMTRKQALKFARANLKLAGQGNKGIGLMNTKNDPTLGEDGISRITVSVDQQAPTKAYLMIEVAPDPSTELNVDLERKSSPMLVVFPVTDPISGNPLQTIHLYPKNVGYVRDPYFFKFGVHPDGTSKRLAGAIFAIYRIENGKKLYLDMSPVTDLRNKWVSTTDPLHDDRVNKFVSDQDGLVNTGERFLPAGEYFFEELQGVPGYEVDAKSRAIKIEIPDSWEDEDGNRRFVLIDGQPMQENFGGVVTPEMISSGYPRVYNYADKQASTTGDQTAGPSTTQLGNHGQDTNGTGTRTPKRQSGYLPLEHHHHHH |
The EcoRI site is underlined.
The XhoI site is underlined.
The cloning artifacts are underlined.